Genetics (contd...)

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» Fondation Jean Dausset - CEPH
» HomoloGene - NCBI
» Human Gene Mutation Database - University of Wales, Cardiff
» Human Genome Center - Lawrence Livermore National Laboratory

 
» Human Genome Epidemiology Network
» Human Genome Mapping Project, UK
» Human Genome Organisation
» Human Genome Sequencing Department - Lawrence Berkeley National Laboratory
» Institute for Genomic Research
» Jablonski's Multiple Congenital Anomaly/Mental Retardation Syndromes - U.S. National Library of Medicine
» Laboratory of Population Genetics
» LocusLink
» Map Viewer - NCBI
» Max Planck Institute for Molecular Genetics
» National Center for Genome Resources
» National Institute of Genetics (Japan)
» National Newborn Screening and Genetics Resource Center - University of Texas at San Antonio
» National Organization for Rare Disorders - Index of Rare Diseases
» National Organization for Rare Disorders - Rare Disease Database
» NCBI BLAST
» NCBI Reference Sequence (RefSeq)
» OMIM - Online Mendelian Inheritance in Man
» ORF Finder (Open Reading Frame Finder) - NCBI
» Orphanet [Français]
» Orphanet - Enfermedades raras - Medicamentos huérfanos [Español]
» Orphanet - Malattie rare - Farmaci orfani [Italiano]
» Orphanet - Rare diseases - Orphan drugs
» Orphanet - seltene Krankheiten - Medikamente für seltene Krankheiten [Deutsch]
» RIKEN Genomic Sciences Center
» SAGEmap - NCBI
» SKY/M-FISH/CGH
» Spidey - mRNA to genomic alignment - NCBI
» Stanford DNA Sequencing and Technology Center - Stanford University
» Stanford Human Genome Center - Stanford University
» Submit to GenBank - NCBI
» UCSC Genome Browser
» UniGene - NCBI
» UniSTS - NCBI
» VecScreen - NCBI
» Wellcome Trust Sanger Institute

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